Zobrazeno 1 - 10
of 935
pro vyhledávání: '"Kruisselbrink A"'
Autor:
Hans Gelderblom, Peter A van Veelen, Noel de Miranda, Arnoud H de Ru, Judith V M G Bovée, Dina Ruano, Marieke Ijsselsteijn, Manon van der Ploeg, Siddh van Oost, Debora M Meijer, Jessica P Roelands, I H Briaire-de Bruijn, B E van den Akker, A B Kruisselbrink, P M Wijers-Koster, S W Lam, R T N Tjokrodirijo, M A J van de Sande, M L Kuijjer
Publikováno v:
BMJ Oncology, Vol 3, Iss 1 (2024)
Objective Osteosarcoma is the most common primary bone sarcoma. About 50% of patients develop metastatic disease and their 5-year survival lingers at around 20%–30%. T cell checkpoint blockade immunotherapies have revolutionised cancer treatment in
Externí odkaz:
https://doaj.org/article/f7ac0bc0200f4326baebbac92a871b2d
Autor:
Beauchamp, Marla, Kirkwood, Renata, Duong, MyLinh, Ho, Terence, Raina, Parminder, Kruisselbrink, Rebecca, Jones, Aaron, Girolametto, Carla, Costa, Andrew
Publikováno v:
In The American Journal of Medicine October 2024 137(10):990-1000
Autor:
Engel, Jasper1 MESE@efsa.europa.eu, Kruisselbrink, Johannes W.1, van Voorthuijsen, Tijmen1, de Boer, Waldo J.1, van Lenthe, Marco S.1, van Donkersgoed, Gerda2, McKeon, Hannah P.2, Zwartsen, Anne2, van Klaveren, Jacob D.2
Publikováno v:
EFSA Supporting Publications. Aug2024, Vol. 21 Issue 8, p1-71. 71p.
Autor:
van Klaveren, Jacob D.1 MESE@efsa.europa.eu, Kruisselbrink, Johannes W.2, Engel, Jasper2, van Voorthuijsen, Tijmen2, van Lenthe, Marco S.2, de Boer, Waldo J.2, van Donkersgoed, Gerda1, McKeon, Hannah P.1, Zwartsen, Anne1
Publikováno v:
EFSA Supporting Publications. Jul2024, Vol. 21 Issue 7, p1-54. 54p.
Autor:
Lisa W. Rodenburg, Mieke Metzemaekers, Isabelle S. van der Windt, Shannon M. A. Smits, Loes A. den Hertog-Oosterhoff, Evelien Kruisselbrink, Jesse E. Brunsveld, Sabine Michel, Karin M. de Winter-de Groot, Cornelis K. van der Ent, Ralph Stadhouders, Jeffrey M. Beekman, Gimano D. Amatngalim
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-15 (2023)
Abstract The nasal and bronchial epithelium are unified parts of the respiratory tract that are affected in the monogenic disorder cystic fibrosis (CF). Recent studies have uncovered that nasal and bronchial tissues exhibit intrinsic variability, inc
Externí odkaz:
https://doaj.org/article/a3543cd790b84d62a839330093785ed4
Autor:
Filippo Pinto e Vairo, Jennifer L. Kemppainen, Carolyn R. Rohrer Vitek, Denise A. Whalen, Kayla J. Kolbert, Kaitlin J. Sikkink, Sarah A. Kroc, Teresa Kruisselbrink, Gabrielle F. Shupe, Alyssa K. Knudson, Elizabeth M. Burke, Elle C. Loftus, Lorelei A. Bandel, Carri A. Prochnow, Lindsay A. Mulvihill, Brittany Thomas, Dale M. Gable, Courtney B. Graddy, Giovanna G. Moreno Garzon, Idara U. Ekpoh, Eva M. Carmona Porquera, Fernando C. Fervenza, Marie C. Hogan, Mireille El Ters, Kenneth J. Warrington, John M. Davis, Matthew J. Koster, Amir B. Orandi, Matthew L. Basiaga, Adrian Vella, Seema Kumar, Ana L. Creo, Aida N. Lteif, Siobhan T. Pittock, Peter J. Tebben, Ejigayehu G. Abate, Avni Y. Joshi, Elizabeth H. Ristagno, Mrinal S. Patnaik, Lisa A. Schimmenti, Radhika Dhamija, Sonia M. Sabrowsky, Klaas J. Wierenga, Mira T. Keddis, Niloy Jewel J. Samadder, Richard J. Presutti, Steven I. Robinson, Michael C. Stephens, Lewis R. Roberts, William A. Faubion, Sherilyn W. Driscoll, Lily C. Wong-Kisiel, Duygu Selcen, Eoin P. Flanagan, Vijay K. Ramanan, Lauren M. Jackson, Michelle L. Mauermann, Victor E. Ortega, Sarah A. Anderson, Stacy L. Aoudia, Eric W. Klee, Tammy M. McAllister, Konstantinos N. Lazaridis
Publikováno v:
Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-2 (2024)
Externí odkaz:
https://doaj.org/article/7330cbbda97649539c05138a79d450aa
Autor:
Filippo Pinto e Vairo, Jennifer L. Kemppainen, Carolyn R. Rohrer Vitek, Denise A. Whalen, Kayla J. Kolbert, Kaitlin J. Sikkink, Sarah A. Kroc, Teresa Kruisselbrink, Gabrielle F. Shupe, Alyssa K. Knudson, Elizabeth M. Burke, Elle C. Loftus, Lorelei A. Bandel, Carri A. Prochnow, Lindsay A. Mulvihill, Brittany Thomas, Dale M. Gable, Courtney B. Graddy, Giovanna G. Moreno Garzon, Idara U. Ekpoh, Eva M. Carmona Porquera, Fernando C. Fervenza, Marie C. Hogan, Mireille El Ters, Kenneth J. Warrington, John M. Davis, Matthew J. Koster, Amir B. Orandi, Matthew L. Basiaga, Adrian Vella, Seema Kumar, Ana L. Creo, Aida N. Lteif, Siobhan T. Pittock, Peter J. Tebben, Ejigayehu G. Abate, Avni Y. Joshi, Elizabeth H. Ristagno, Mrinal S. Patnaik, Lisa A. Schimmenti, Radhika Dhamija, Sonia M. Sabrowsky, Klaas J. Wierenga, Mira T. Keddis, Niloy Jewel J. Samadder, Richard J. Presutti, Steven I. Robinson, Michael C. Stephens, Lewis R. Roberts, William A. Faubion, Sherilyn W. Driscoll, Lily C. Wong-Kisiel, Duygu Selcen, Eoin P. Flanagan, Vijay K. Ramanan, Lauren M. Jackson, Michelle L. Mauermann, Victor E. Ortega, Sarah A. Anderson, Stacy L. Aoudia, Eric W. Klee, Tammy M. McAllister, Konstantinos N. Lazaridis
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-10 (2023)
Abstract Background In the United States, rare disease (RD) is defined as a condition that affects fewer than 200,000 individuals. Collectively, RD affects an estimated 30 million Americans. A significant portion of RD has an underlying genetic cause
Externí odkaz:
https://doaj.org/article/379d322058a142068b8b67a35317dec9
Publikováno v:
In Journal of PeriAnesthesia Nursing April 2023 38(2):186-192
Autor:
Mohananey, Akanksha, Tseng, Andrew S., Julakanti, Raghav R., Gonzalez-Bonilla, Hilda M., Kruisselbrink, Teresa, Prochnow, Carri, Rodman, Sandra, Lin, Grace, Redfield, Margaret M., Rosenbaum, Andrew N., Pereira, Naveen L.
Publikováno v:
In Genetics in Medicine March 2023 25(3)
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